Fortrea

Job Overview:Line manage PSS staff including performance reviews human resource issues and assist Senior PSS Management in assigning resources to projects.Manage the overall PSS operations associated with products including the entire adverse events process; which may include safety d

Job Overview:Line manage PSS staff including performance reviews human resource issues and assist Senior PSS Management in assigning resources to projects.Manage the overall PSS operations associated with products including the entire adverse events process; which may include safety d

Develop in conjunction with the Global Feasibility Lead the initial site list for feasibility and site identificationFull oversight of the Feasibility/Site identification process: survey development and programming local resource training and oversight oversight of site outreach proce

Develop in conjunction with the Global Feasibility Lead the initial site list for feasibility and site identificationFull oversight of the Feasibility/Site identification process: survey development and programming local resource training and oversight oversight of site outreach proce

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:The In-House Clinical Research Associate (IHCRA I) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA I shall reflect their experience and level of contribution wh

Job Overview:The In-House Clinical Research Associate (IHCRA I) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA I shall reflect their experience and level of contribution wh

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Serve as a member of the project team with primary responsibility for clinical data review query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications and project timelines and producti

Job Overview:Serve as a member of the project team with primary responsibility for clinical data review query generation / resolution and reconciliation to support the delivery of clinical data according to client quality and integrity specifications and project timelines and producti

Join Our Proposal Management Team! - Hybrid Role - Leeds UK Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehensi

Join Our Proposal Management Team! - Hybrid Role - Leeds UK Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehensi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

Summary of Responsibilities:Works with internal teams to progress quality issues in QMS.Tracks timeliness of cases in QMS.Supports teams in creation of CAPAs.Maintains strong working knowledge of QMS.Interacts with QA Lead Manager and above as required for quality issue case progressi

***Must possess at least 3-5 years of people management/direct reports experience.***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Clinical Operations Supervisor II to int

***Must possess at least 3-5 years of people management/direct reports experience.***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Clinical Operations Supervisor II to int

Join Our Proposal Management Team! Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehension and writing skills to

Join Our Proposal Management Team! Are you fluent in English passionate about clear professional communication and ready to grow your career in proposal development Were looking for a detail-oriented collaborative individual with excellent English comprehension and writing skills to

Summary of Responsibilities:Respond to medical information queries (In French)/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and report Adverse Drug Reaction in timelines (according to the regulations a

Summary of Responsibilities:Respond to medical information queries (In French)/product quality complaints/general queries that may be received over the telephone call email fax etc.Receive information record and report Adverse Drug Reaction in timelines (according to the regulations a

Fortrea is seeking Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with oncology background. CRA experience is required. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manage

Fortrea is seeking Clinical Team Leads to join our FSP team! We are seeking experienced CTLs with oncology background. CRA experience is required. Job Overview:Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manage

***Must possess extensive GCP experience and the ability to liaison cross-functionally***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking an Operational Quality Specialist to

***Must possess extensive GCP experience and the ability to liaison cross-functionally***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking an Operational Quality Specialist to

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Research Nurse (RNs LPNs) and Paramedics to interact directly with our healthy volunteer participants while learning to read

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Research Nurse (RNs LPNs) and Paramedics to interact directly with our healthy volunteer participants while learning to read

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Research Nurse / Open to RNs LPNs or Paramedics to lead and support our Clinical Pharmacology Start-up team in initiating Ear

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Research Nurse / Open to RNs LPNs or Paramedics to lead and support our Clinical Pharmacology Start-up team in initiating Ear

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

Are you passionate about making a real impact on global healthcare We are seeking an exceptional Sr Biostatistics Manager (RWE) to join our dynamic Consulting team dedicated to advancing Real-World Evidence (RWE) this pivotal role youll be at the forefront of delivering high-profile

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Clinical Operations Supervisor to interact directly with our healthy volunteer participants while learning to read clinical r

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Clinical Operations Supervisor to interact directly with our healthy volunteer participants while learning to read clinical r